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exo·cyc·lic (ek″so-sikґlik) (-siґklik) denoting one or more atoms attached to a ring structure but outside it.Medical dictionary. 2011.
exocyclic — ex·o·cy·clic (ĕk sō sīʹklĭk, sĭkʹlĭk) adj. External to a chemical ring structure: an exocyclic double bond. * * * … Universalium
exocyclic bond — egzociklinis ryšys statusas T sritis chemija apibrėžtis Dvigubasis ryšys tarp žiedo ir pakaito atomų. atitikmenys: angl. exocyclic bond; exocyclic double bond rus. экзоциклическая связь … Chemijos terminų aiškinamasis žodynas
exocyclic double bond — egzociklinis ryšys statusas T sritis chemija apibrėžtis Dvigubasis ryšys tarp žiedo ir pakaito atomų. atitikmenys: angl. exocyclic bond; exocyclic double bond rus. экзоциклическая связь … Chemijos terminų aiškinamasis žodynas
exocyclic — adjective Date: 1913 situated outside of a ring in a chemical structure … New Collegiate Dictionary
exocyclic — adjective (of a cyclic compound) not forming part of, or not attached to the ring … Wiktionary
exocyclic — … Useful english dictionary
Oligonucleotide synthesis — is the chemical synthesis of relatively short fragments of nucleic acids with defined chemical structure (sequence). The technique is extremely useful in current laboratory practice because it provides a rapid and inexpensive access to custom… … Wikipedia
Anomeric effect — In organic chemistry, the anomeric effect or Edward Lemieux effect is a stereoelectronic effect that describes the tendency of heteroatomic substituents adjacent to a heteroatom within a cyclohexane ring to prefer the axial orientation instead of … Wikipedia
Nucleoside phosphoramidite — Protected 2 deoxynucleoside phosphoramidites. Nucleoside phosphoramidites are derivatives of natural or synthetic nucleosides. They are used to synthesize oligonucleotides, relatively short fragments of nucleic acid and their analogs. Nucleoside… … Wikipedia
Danishefsky Taxol total synthesis — overview from raw material perspective The Danishefsky Taxol total synthesis in organic chemistry is an important third Taxol synthesis published by the group of Samuel Danishefsky in 1996 [1] two years after the first two efforts … Wikipedia
